Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs
Job Summary
Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs.
Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials.
Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations.
Matching Summary
Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs.